Cardoso Váldina Solimar Lopes, Valente-Amaral Anderson, Monteiro Rayan Fidel Martins, Meira Clarina Loius Silva, de Meira Natália Silva, da Silva Milton Nascimento, Pinheiro João de Jesus Viana, Bastos Gilmara de Nazareth Tavares, Felício João Soares, Yamada Elizabeth Sumi
Experimental Neuropathology Laboratory, João de Barros Barreto University Hospital, Federal University of Pará, Belém, Brazil.
Oncology Research Center and Graduate Program in Oncology and Medical Sciences, João de Barros Barreto University Hospital, Federal University of Pará, Belém, Brazil.
Front Neurosci. 2024 Feb 21;18:1351718. doi: 10.3389/fnins.2024.1351718. eCollection 2024.
Parkinson's disease affects 2% of the population aged over 65 years and is the second most common neurodegenerative disorder in the general population. The appearance of motor symptoms is associated with the degeneration of dopaminergic neurons in the nigrostriatal pathway. Clinically significant nonmotor symptoms are also important for severe disability with disease progression. Pharmacological treatment with levodopa, which involves dopamine restitution, results in a temporary improvement in motor symptoms. Among the mechanisms underlying the pathogenesis of the disease are exacerbated oxidative stress, mitochondrial dysfunction, and neuroinflammation. A phytochemical prospecting study showed that the aqueous extract of the leaves from (Melineaceae), known as mahogany, has polyphenols with antioxidant and anti-inflammatory capacity in a significantly higher percentage than leaf extracts from other Amazonian plants. Furthermore, the antioxidant and anti-inflammatory capacity of aqueous extract of mahogany leaf has already been demonstrated in an model. In this study, we hypothesized that the aqueous extract of mahogany leaf (AEML) has a neuroprotective effect in a murine model of Parkinson's disease induced by 6-hydroxidopamine (6-OHDA), due to antioxidant and anti-inflammatory properties of its phenolic compounds.
Mice were treated daily with the mahogany extract at a dose of 50 mg/kg, starting 7 days before 6-OHDA infusion until post-surgery day 7.
The animals from the 6-OHDA/mahogany group, which corresponds to animals injected with the toxin and treated with aqueous extract of the mahogany leaf, presented distinct behavioral phenotypes after apomorphine challenge and were therefore subdivided into 2 groups, 6-OHDA/mahogany F1 and 6-OHDA/mahogany F2. The F1 group showed a significant increase in contralateral rotations, whereas the F2 group did not show rotations after the apomorphine stimulus. In the F1 group, there was an increase, although not significant, in motor performance in the open field and elevated plus maze tests, whereas in the F2 group, there was significant improvement, which may be related to the lesser degree of injury to the nigrostriatal dopaminergic pathway. The TH+ histopathological analysis, a dopaminergic neuron marker, confirmed that the lesion to the nigrostriatal dopaminergic pathway was more pronounced in 6-OHDA/mahogany F1 than in 6-OHDA/mahogany F2. Our main result consisted of signs of improvement in the inflammatory profile in both the F1 and F2 6-OHDA/mahogany groups, such as a lower number of IBA-1+ microglial cells in the ventral striatum and substantia nigra pars compacta and a reduction in GFAP+ expression, an astrocyte marker, in the dorsal striatum. In this study, several bioactive compounds in the aqueous extract of mahogany leaf may have contributed to the observed beneficial effects. Further studies are necessary to better characterize their applicability for treating chronic degenerative diseases with inflammatory and oxidative bases, such as Parkinson's disease.
帕金森病影响2%的65岁以上人群,是普通人群中第二常见的神经退行性疾病。运动症状的出现与黑质纹状体通路中多巴胺能神经元的退化有关。具有临床意义的非运动症状对于疾病进展导致的严重残疾也很重要。左旋多巴的药物治疗涉及多巴胺补充,可使运动症状暂时改善。该疾病发病机制的潜在机制包括氧化应激加剧、线粒体功能障碍和神经炎症。一项植物化学勘探研究表明,桃花心木(楝科)叶子的水提取物含有多酚,其抗氧化和抗炎能力的百分比明显高于其他亚马逊植物的叶子提取物。此外,桃花心木叶水提取物的抗氧化和抗炎能力已在动物模型中得到证实。在本研究中,我们假设桃花心木叶水提取物(AEML)在6-羟基多巴胺(6-OHDA)诱导的帕金森病小鼠模型中具有神经保护作用,这归因于其酚类化合物的抗氧化和抗炎特性。
从6-OHDA注入前7天开始,每天以50mg/kg的剂量用桃花心木提取物治疗小鼠,直至术后第7天。
6-OHDA/桃花心木组的动物,即注射毒素并用桃花心木叶水提取物治疗的动物,在阿扑吗啡激发后表现出不同的行为表型,因此被分为2组,6-OHDA/桃花心木F1组和6-OHDA/桃花心木F2组。F1组对侧旋转显著增加,而F2组在阿扑吗啡刺激后未出现旋转。在F1组中,旷场试验和高架十字迷宫试验中的运动表现有所增加,尽管不显著,而在F2组中,有显著改善,这可能与黑质纹状体多巴胺能通路的损伤程度较轻有关。TH+组织病理学分析是一种多巴胺能神经元标记物,并证实黑质纹状体多巴胺能通路在6-OHDA/桃花心木F1组中的损伤比在6-OHDA/桃花心木F2组中更明显。我们的主要结果是,在6-OHDA/桃花心木F1组和F2组中,炎症特征均有改善迹象,如腹侧纹状体和黑质致密部中IBA-1+小胶质细胞数量减少,以及背侧纹状体中GFAP+表达降低,GFAP是一种星形胶质细胞标记物。在本研究中,桃花心木叶水提取物中的几种生物活性化合物可能促成了观察到的有益效果。有必要进行进一步研究,以更好地确定其在治疗具有炎症和氧化基础的慢性退行性疾病(如帕金森病)中的适用性。